Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001495070 | SCV001699739 | likely benign | Nemaline myopathy 2 | 2019-12-18 | criteria provided, single submitter | clinical testing |